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2019冠状病毒病与静脉血栓栓塞症之间的共同遗传病因及因果关系:来自全基因组跨性状分析和双向孟德尔随机化研究的证据

Shared genetic etiology and causality between COVID-19 and venous thromboembolism: evidence from genome-wide cross trait analysis and bi-directional Mendelian randomization study.

作者信息

Huang Xin, Yao Minhao, Tian Peixin, Wong Jason Y Y, Li Zilin, Liu Zhonghua, Zhao Jie V

出版信息

medRxiv. 2022 Jun 1:2022.05.21.22275413. doi: 10.1101/2022.05.21.22275413.

DOI:10.1101/2022.05.21.22275413
PMID:35665015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9164523/
Abstract

Venous thromboembolism (VTE) occurs in up to one third patients with COVID-19. VTE and COVID-19 may share a common genetic architecture, which has not been clarified yet. To fill this gap, we leveraged summary-level genetic data from the latest COVID-19 host genetics consortium and UK Biobank and examined the shared genetic etiology and causal relationship between COVID-19 and VTE. The cross-trait analysis identified 8, 11, and 7 shared loci between VTE and severe COVID-19, COVID-19 hospitalization, SARS-CoV-2 infection respectively, in 13 genes involved in coagulation and immune function and enriched in the lung. Co-localization analysis identified eight shared loci in and genes. Bi-direction Mendelian randomization suggested that VTE was associated with higher risks of all COVID-19 related traits, and SARS-CoV-2 infection was associated with higher risk of VTE. Our study provided timely evidence and novel insights into the genetic etiology between COVID-19 and VTE.

摘要

静脉血栓栓塞症(VTE)在多达三分之一的新冠病毒病(COVID-19)患者中出现。VTE和COVID-19可能具有尚未明确的共同遗传结构。为填补这一空白,我们利用了来自最新的COVID-19宿主遗传学联盟和英国生物银行的汇总水平遗传数据,并研究了COVID-19与VTE之间的共同遗传病因及因果关系。跨性状分析在分别与严重COVID-19、COVID-19住院治疗、严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染相关的VTE中,确定了8个、11个和7个共享基因座,这些基因座存在于13个参与凝血和免疫功能并在肺部富集的基因中。共定位分析在[具体基因]和[具体基因]中确定了8个共享基因座。双向孟德尔随机化表明,VTE与所有COVID-19相关性状的较高风险相关,而SARS-CoV-2感染与VTE的较高风险相关。我们的研究为COVID-19与VTE之间的遗传病因提供了及时的证据和新的见解。